Showing entry for Intrinsic hand muscle atrophy



                               
General Disease Information
BXGD IdBXGD016245
Disease NameIntrinsic hand muscle atrophy
Disease CUI IdC1864716
MeSH Codes   
Disease Class Name
Semantic TypeFinding
Human Phenotype Ontology Id HP:0040064   HP:0003011  
Human Phenotype Ontology TermAbnormality of limbs; Abnormality of the musculature
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations